Pandyaraj R A, Sathik Mohamed Masoodu K, Maniselvi S, Savitha S, Divya Devi H
Kilpauk Medical College, No.11, Begum Sahib 3rd Street, Mount Road, Chennai, 600 002 India.
Kilpauk Medical College, 32/615 F2, 24th Cross Street, Shanthi Nagar, Palayamkottai, Tirunelveli, 627 002 India.
Indian J Surg. 2015 Apr;77(Suppl 1):49-51. doi: 10.1007/s12262-014-1118-2. Epub 2014 Jun 17.
Langerhans cell histiocytosis (LCH) is a rare disease of antigen presenting cells and involvement of thyroid is really uncommon. The thyroid if involved is usually seen in multisystem disease but isolated thyroid involvement is very rare. The diagnosis of Langerhans cell histiocytosis of the thyroid is very challenging due to its rarity and is usually misdiagnosed as benign goiters, undifferentiated carcinoma, lymphoma, etc. Management of Langerhans cell histiocytosis of the thyroid also remains controversial. Prognosis in an isolated Langerhans cell histiocytosis of the thyroid is usually good but as it may precede a multisystem involvement, prolonged follow-up is required. We present a rare case of Langerhans cell histiocytosis of the thyroid, with variable diagnoses on fine needle aspiration cytology.
朗格汉斯细胞组织细胞增多症(LCH)是一种罕见的抗原呈递细胞疾病,甲状腺受累极为罕见。甲状腺若受累,通常见于多系统疾病,但孤立性甲状腺受累非常罕见。甲状腺朗格汉斯细胞组织细胞增多症的诊断极具挑战性,因其罕见,通常被误诊为良性甲状腺肿、未分化癌、淋巴瘤等。甲状腺朗格汉斯细胞组织细胞增多症的治疗也仍存在争议。孤立性甲状腺朗格汉斯细胞组织细胞增多症的预后通常良好,但由于其可能先于多系统受累,需要长期随访。我们报告一例罕见的甲状腺朗格汉斯细胞组织细胞增多症病例,细针穿刺细胞学检查有多种诊断结果。